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Weaver, J.D., Recio III, A., Grenning, A.J. and Tunge, J.A. (2011) Transition metal-catalyzed decarboxylative allylation and benzylation reactions. Chemical Reviews, 111, 1846-1913. Trivedi, R. and Tunge, J.A. (2009) Regioselective iron-catalyzed decarboxylative allylic etherification. Organic Letters, 11, 5650-5652. Goossen, L.J., Goossen, K., Rodriguez, N., Blanchot, M., Linder, C. and Zimmermann, B. (2008) New catalytic trans-formations of carboxylic acids. Pure and Applied Chemical, 80, 1725-1733.

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  • 标题: 钯催化烯丙基碳酸肟脱羧合成烯丙基肟Palladium-Catalyzed Allyl Oxime from Allyloxycarbonyl Oxime

    作者: 蔡波, 李文广, 皮少锋, 孙汉州

    关键字: , 脱羧, 烯丙基肟Palladium, Decarboxylation, Allyl Oxime

    期刊名称: 《Journal of Organic Chemistry Research》, Vol.3 No.1, 2015-03-31

    摘要: 肟类化合物是一类重要的含氮化合物,广泛存在于天然产物、药物和活性物质的一种单元结构,是一种重要的有机合成中间体。研究了在钯催化条件下烯丙基碳酸肟脱羧反应,发展了一种反应条件温和,原料便宜易得,对环境友好的合成烯丙基肟方法,在常温下,以Pd(PPh3)4为催化剂,DCM为溶剂的反应体系中,反应8分钟就可以得到较高收率的烯丙基肟。并对该反应可能的机理进行了探讨。 Oximes, which are important classes of nitrogen compounds, are ubiquitous in natural products, drugs as well as materials, and are important intermediates in organic synthesis. We have devel-oped a mild and convenient protocol for the synthesis of allyl oximes. In the presence of Pd(PPh3)4 and DCM, allyloxycarbonyl oximes successfully underwent decaboxylate reaction at room tem-perature to afford the corresponding allyl oximes in moderate good yields in eight minutes. And the possible mechanism of the reaction was discussed.

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